HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545622Generated: October 25, 2026
2-Phenylethanol → 2-[4-(6-Methyl-benzothiazol-2-yloxy)-phenyl]-ethanol
https://huagongshe.com/reaction/545622
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | Isopropyl Acetate | HCID 7915 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-6-methylbenzothiazole | HCID 2049866 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[4-(6-Methyl-benzothiazol-2-yloxy)-phenyl]-ethanol | HCID 67205666 | 63% |
Reaction Steps
To a solution of phenethyl alcohol (3.15 g, 22.86 mmol) and K2CO3 (5.26 g, 38.1 mmol) in CH3CN (35 mL) was added 2-chloro-6-methylbenzthiazole (3.5 g, 19.1 mmol). The reaction mixture was heated at 80° C. for 16 h. To the reaction mixture was added 1 N NaOH (30 mL) and isopropyl acetate (40 mL). The layers were separated and the aqueous layer was extracted with isopropyl acetate (2×30 mL). The combined organic layers were dried (Na2SO4), filtered and concentrated. The resulting residue was purified by silica gel flash chromatography (20% to 90% EtOAc in hexanes) to afford the title compound (3.4 g, 63%). 1H NMR (500 MHz, CDCl3): 7.61 (d, J=8.3 Hz, 1H), 7.47 (s, 1H), 7.33-7.28 (m, 4H), 7.20 (d, J=8.3 Hz, 1H), 3.87 (br s, 2H), 2.90 (t, J=6.6 Hz, 2H), 2.44 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935725B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-8b5994e7e0344801bc9ae553da8172d2 |
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| Source note | uspto-grants-2011_05 |
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